DisGeNET - a database of gene-disease associations

Source: GWASDB

Variants associated to the Gene: LRP1 ×

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Gene

Disease

Variant

Source

DSI _v

DPI _v

pLI

Consequence

AF_EXOME

AF_GENOME

Variant	Gene	DSI _v	DPI _v	Chr	Position	Consequence	Alleles	Class	AF EXOME	AF GENOME	Num. diseases
rs34660894	LRP1 ; STAT6			12	57129111	intron variant	G/A	snv	2.3E-03	1.0E-02	5
rs11172113	LRP1	0.882	0.080	12	57133500	intron variant	T/C	snv		0.42	4
rs34614287	LRP1			12	57155352	3 prime UTR variant	C/G	snv		6.8E-04	4
rs34630693	LRP1			12	57212472	missense variant	C/A;T	snv	1.2E-05; 2.0E-05		4
rs1466535	LRP1	0.790	0.160	12	57140687	intron variant	G/A;C	snv			1
rs34574998	LRP1			12	57154581	synonymous variant	T/C	snv	2.3E-02	4.0E-02	1
rs35161844	LRP1			12	57184057	intron variant	C/T	snv	7.2E-03	2.8E-02	1
rs35599705	LRP1			12	57175044	intron variant	G/A	snv		1.3E-02	1
rs35253246	LRP1			12	57155077	3 prime UTR variant	T/G	snv		5.2E-02	1
rs34576916	LRP1			12	57209288	intron variant	C/G	snv		4.0E-04	1
rs7488264	MIR1228 ; LRP1			12	57194266	intron variant	A/G;T	snv			1